Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1981-11-22
pubmed:abstractText
Purified hemagglutinin and fusion glycoproteins of measles virus either in soluble form or inserted in artifical membranes bind to human peripheral blood lymphocytes and induce cell-mediated cytotoxicity (CMC) in a dose-response fashion. Both autologous and heterologous noninfected target cells are lysed in vitro. The expression of CMC is not inhibited by anti-measles virus antibody added to lymphocytes previously exposed to viral glycoproteins. THe killer lymphocytes are Fc receptor positive, both erythrocyte-rosetting and non-erythrocyte-rosetting, as assessed by both positive and negative selection experiments. The induction of nonspecific CMC by viral glycoproteins either in the soluble state or inserted into artificial membranes could be segregated from the CMC associated with whole virions. First, on kinetics studies, purified viral glycoproteins induced CMC more rapidly than did whole virus. Second, viral glycoprotein-produced response occurred in the absence of detectable release of interferon into the culture medium, whereas CMC activity due to whole virions was associated with interferon release. The fact that purified measles virus glycoproteins integrated into artificial membrane bilayers were as efficient as their soluble counterparts in inducing CMC suggests that the hydrophobic portion of the glycoproteins was not involved in the induction and expression of the lytic activity. Purified glycoproteins from lymphocytic choriomeningitis virus behave similarly, although this virus is unrelated to measles virus. It is inferred that interferon-independent CMC induced by viral glycoproteins might account for some of the biological reactions occurring early in the control of a viral infection.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-14907713, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-153888, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-164055, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-177712, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-186554, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-221611, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-300306, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-302316, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-4130071, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-4360138, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-489977, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-5432063, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-566386, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-589672, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-6154245, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-6154760, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-6158744, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-6251708, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-650156, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-685174, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-6928644, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-7288404, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-7381212, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-7384752, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-761939, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-830751, http://linkedlifedata.com/resource/pubmed/commentcorrection/7276828-92183
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0022-1007
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
154
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
840-55
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1981
pubmed:articleTitle
In vitro generation of human cytotoxic lymphocytes by virus. Viral glycoproteins induce nonspecific cell-mediated cytotoxicity without release of interferon.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't